嵌合抗原受体
免疫疗法
淋巴瘤
医学
CD19
免疫系统
癌症研究
多发性骨髓瘤
T细胞
免疫学
抗原
作者
Regina M. Young,Nils W Engel,Ugur Uslu,Nils Wellhausen,Carl H. June
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2022-04-12
卷期号:: OF1-OF14
标识
DOI:10.1158/2159-8290.cd-21-1683
摘要
CD19- and B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cells have enabled unprecedented responses in a subset of refractory patients with B-cell and plasma cell malignancies, leading to their approval by the FDA for the treatment of leukemia, lymphoma, and myeloma. These "living drugs" can become part of a synthetic immune system, persisting at least a decade in some patients. However, despite this tremendous impact, significant unmet treatment needs remain for patients with hematologic malignancies and solid cancers. In this perspective, we highlight recent innovations that advance the field toward production of a more potent and universal cellular immunotherapy of the future. Next-generation CAR T cells will incorporate advances in gene engineering and synthetic biology to enhance functionality and persistence, and reduce treatment-associated toxicities. The combination of autologous CAR T cells with various allogeneic cell treatment strategies designed to target the immunosuppressive tumor microenvironment will broaden the impact of future CAR T-cell therapies.
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